Quality Engineer II — Medical Device (Onsite — Spencer, IN) Contract

Job Summary:  

The Quality Engineer II develops, establishes and maintains quality engineering methodologies, systems, and practices which meet internal, customer, and regulatory requirements. They Serve as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. They provide focused quality engineering support within new product development, operational, or system/services support. Functional Engineering Roles include Design Assurance, Operations Quality, Software Engineering, Supplier Assurance, Product Analysis, Metrology, Microbiologist, Chemist. 

Responsibilities:  

• Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements. 
  

• Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. 
  

• Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices. 
  

• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. 
  

• Assure in the development and execution of streamlined business systems which effectively identify and resolve quality issues. 
  

Quality Systems Duties and Responsibilities: 

• Build Quality into all aspects of their work by maintaining compliance to all quality requirements. 
  

Qualifications: 

• 2 - 4 Years with BS; 1-2 Years with MS 
  

• Must be an analytical thinker 
  

• Organized with attention to detail 
  

• Technical writing experience 
  

Other Details: 

• Schedule: 08:00 AM - 04:30 PM (Flexible) 
  

• Work Setup: Onsite in Spencer, IN 
  

• Contract Length: 12 Months 
  

• Start Date: 8/25/2025